Canonical Allele Identifier: CA1619250123

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655999C= , CM000668.2:g.31655999C=	GRCh38
NC_000006.11:g.31623776C= , CM000668.1:g.31623776C=	GRCh37
NC_000006.10:g.31731755C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.33C= (APOM) MANE Select	ENSP00000365081.3:p.Tyr11=
ENST00000375916.3:c.33C= (APOM)	ENSP00000365081.3:p.Tyr11=
ENST00000375918.6:c.-102-473C= (APOM)	ENSP00000365083.2:n.-102-473C=
ENST00000375920.8:c.-102-473C= (APOM)	ENSP00000365085.4:n.-102-473C=
NM_001256169.1:c.-102-473C= (APOM)	NP_001243098.1:n.-102-473C=
NM_019101.2:c.33C= (APOM)	NP_061974.2:p.Tyr11=
NR_045828.1:n.143-473C= (APOM)
XM_006715150.2:c.-71C= (APOM)	XP_006715213.1:n.-71C=
XM_011514895.1:c.-13-4223G= (BAG6)	XP_011513197.1:n.-13-4223G=
XM_006715150.3:c.-71C= (APOM)	XP_006715213.1:n.-71C=
XM_017011279.2:c.-13-4223G= (BAG6)	XP_016866768.1:n.-13-4223G=
XM_024446545.1:c.-14+1765G= (BAG6)	XP_024302313.1:n.-14+1765G=
NM_019101.3:c.33C= (APOM) MANE Select	NP_061974.2:p.Tyr11=
NM_001256169.2:c.-102-473C= (APOM)	NP_001243098.1:n.-102-473C=
NR_045828.2:n.149-473C= (APOM)